Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
1.
Fish Shellfish Immunol ; 93: 1067-1075, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31386909

ABSTRACT

Fishmeal is the main source of protein in the shrimp feed industry and is normally derived from trash fish. As such, the production of fishmeal has an adverse effect on the marine environment by taking away small and juvenile fish, leading to depletion of marine species. There is a need for alternative sources of protein which will substitute fishmeal in the aquaculture industry. This study evaluated the components and nutritional efficacy of bioflocs, which were used to substitute fishmeal protein. The effect of bioflocs diets on growth performance, survival rate, and immune response in shrimp compared to normal fishmeal feed were determined. Bioflocs were harvested from the shrimp ponds (C:N ratio >12:1) at Shrimp Village, Chaiya district, Surat Thani, Thailand. The total protein in bioflocs was about 48% and the total lipid was about 5% (dried weight) and the percentages of essential amino acids (EAA) and fatty acids (EFA) in bioflocs were similar to those of fishmeal feed. Shrimp fed with the different dietary bioflocs feed regimens [% to replace fishmeal; 0% (B0), 25% (B25), 50% (B50), 75% (B75), and 100% (B100)] for 42 days revealed that all growth parameters were almost similar to those of the control shrimp (shrimp fed with normal fishmeal, B0) including final body weight, weight gain, specific growth rate, and feed conversion ratio. Remarkably, the survival rates, the levels of immune parameters, and expression of immune genes (proPO-I, PEN-4 and dicer) were significantly higher in bioflocs fed shrimp, especially in B25 and B50 shrimp. Moreover, B25 and B50 bioflocs fed shrimp showed notably increased survival rates following Vibrio parahaemolyticus (V. parahaemolyticus) infection. In conclusion, the present study demonstrates that shrimp survival and immunity are enhanced by biofiocs substituted fishmeal. Significantly, the bioflocs diets activated the immune response to prevent V. parahaemolyticus infection.


Subject(s)
Animal Feed/analysis , Immunity, Innate/drug effects , Penaeidae/immunology , Protective Agents/pharmacology , Vibrio parahaemolyticus/physiology , Animals , Aquaculture , Diet , Dietary Supplements/analysis , Dose-Response Relationship, Drug , Penaeidae/microbiology , Protective Agents/administration & dosage
2.
Article in English | MEDLINE | ID: mdl-38061253

ABSTRACT

Seawater (SW)-acclimated Nile tilapia, Oreochromis niloticus, can tolerate up to 30 g.L-1 SW but rarely produce offspring. The embryos of SW-acclimated O. niloticus survived equally well from 0- to 10-g.L-1 environment but not under 20-g. L-1. However, when the embryos were incubated under 10 g.L-1 during days 0-3, and then the salinity was suddenly shifted to and maintained at 20 g.L-1 during days 4-6, their survival rate was comparable to those incubated under 0 and 10 g.L-1. To elucidate a molecular adaptation of the embryos that survived different salinity environments, the proteomic profiles of the newly hatched embryos, or early larvae, hatched under 0 g.L-1, 10 g.L-1, and those being incubated at 10 g.L-1 during days 0-3 followed at 20 g.L-1 during days 4-6 were compared. Total proteins extracted from the samples were identified with a gel-free shot-gun proteomics approach using the Nile tilapia protein database. The early larvae from the three groups expressed 2295 proteins, and 279 proteins showed statistically different expressions among groups. Downregulation of the 182 proteins in the larvae hatched under 10 and 20 g.L-1 was found to include 22 proteins that are responsible for cellular responses to osmotic stress. This adaptation may be a crucial factor in reducing cellular metabolism and ion transport between the intra- and extra-cellular environment to stabilize cellular osmolality. In addition, some of these proteins suppress cellular damage from oxygen free radicals generated from the osmotic stress. Eighty-seven proteins significantly changed in the larvae hatched under 20 g.L-1 were clustered. Nineteen of the cellular stress response proteins, which were considered to be mortality induction, were described.


Subject(s)
Cichlids , Animals , Osmotic Pressure , Proteomics , Salinity , Acclimatization
3.
BMC Vet Res ; 9: 189, 2013 Sep 30.
Article in English | MEDLINE | ID: mdl-24074037

ABSTRACT

BACKGROUND: Abdominal segment deformity disease (ASDD) of cultivated whiteleg shrimp Penaeus (Litopenaeus) vannamei causes economic loss of approximately 10% in affected specimens because of the unsightliness of distorted abdominal muscles. It is associated with the presence of viral-like particles seen by electron microscopy in the ventral nerve cords of affected shrimp. Thus, shotgun cloning was carried out to seek viral-like sequences in affected shrimp. RESULTS: A new retrovirus-like element of 5052 bp (named abdominal segment deformity element or ASDE) was compiled by shotgun cloning and 3' and 5' RACE using RNA and DNA extracted from ventral nerve cords of ASDD shrimp. ASDE contained 7 putative open reading frames (ORF). One ORF (called the PENS sub-domain), had a deduced amino acid (aa) sequence homologous to the GIY-YIG endonuclease domain of penelope-like retrotransposons while two others were homologous to the reverse transcriptase (RT) and RNaseH domains of the pol gene of non-long terminal repeat (non-LTR) retrotransposons (called the NLRS sub-domain). No single amplicon of 5 kb containing both these elements was obtained by PCR or RT-PCR from ASDD shrimp. Subsequent analysis indicated that PENS and NLRS were not contiguous and that NLRS was a host genetic element. In situ hybridization using a dioxygenin-labeled NLRS probe revealed that NLRS gave positive reactions in abdominal-ganglion neurons of ASDD shrimp but not normal shrimp. Preliminary analysis indicated that long-term use of female broodstock after eyestalk ablation in the hatchery increased the intensity of RT-PCR amplicons for NLRS and also the prevalence of ASDD in mysis 3 offspring of the broodstock. The deformities persist upon further cultivation until shrimp harvest but do not increase in prevalence and do not affect growth or survival. CONCLUSIONS: Our results suggested that NLRS is a shrimp genetic element associated with ASDD and that immediate preventative measures could include shorter-term use of broodstock after eyestalk ablation and/or discard of broodstock that give strong RT-PCR reactions for NLRS. In the longer term, it is recommended, if possible, that currently used, domesticated shrimp lines be selected for freedom from NLRS. The molecular tools developed in this work will facilitate the management and further study of ASDD.


Subject(s)
Penaeidae , Retroelements/genetics , Retroviridae/genetics , Amino Acid Sequence , Animals , Aquaculture , Blotting, Southern , Cloning, Molecular , Female , Larva , Male , Molecular Sequence Data , Penaeidae/ultrastructure , Phylogeny , Reverse Transcriptase Polymerase Chain Reaction
4.
BMC Vet Res ; 9: 33, 2013 Feb 15.
Article in English | MEDLINE | ID: mdl-23414329

ABSTRACT

BACKGROUND: Persistent infection of Penaeus stylirostris densovirus (PstDNV) (also called IHHNV) and its non-infectious inserts in the black tiger shrimp, Penaeus monodon (P. monodon) genome are commonly found without apparent disease. Here, we introduced the method of multiplex PCR in order to differentiate shrimp with viral inserts from ones with the infectious virus. The method allowed us to study the effect of pre-infection of IHHNV, in comparison to IHHNV inserts, on WSSV resistance in P. monodon. RESULTS: A multiplex PCR system was developed to amplify the entire IHHNV genome, ensuring the accurate diagnosis. Field samples containing IHHNV DNA templates as low as 20 pg or equivalent 150 viral copies can be detected by this method. By challenging the two groups of diagnosed shrimp with WSSV, we found that shrimp with IHHNV infection and those with viral inserts responded to WSSV differently. Considering cumulative mortality, average time to death of shrimp in IHHNV-infected group (day 14) was significantly delayed relative to that (day 10) of IHHNV-inserted group. Real-time PCR analysis of WSSV copy number indicated the lower amount of WSSV in the IHHNV-infected group than the virus-inserted group. The ratio of IHHNV: WSSV copy number in all determined IHHNV-infected samples ranged from approximately 4 to 300-fold. CONCLUSION: The multiplex PCR assay developed herein proved optimal for convenient differentiation of shrimp specimens with real IHHNV infection and those with insert types. Diagnosed shrimp were also found to exhibit different WSSV tolerance. After exposed to WSSV, the naturally pre-infected IHHNV P. monodon were less susceptible to WSSV and, consequently, survived longer than the IHHNV-inserted shrimp.


Subject(s)
Densovirus/physiology , Parvoviridae Infections/veterinary , Penaeidae/virology , Animals , Multiplex Polymerase Chain Reaction/veterinary , Parvoviridae Infections/virology , Real-Time Polymerase Chain Reaction/veterinary
5.
Zootaxa ; 5293(3): 581-595, 2023 May 23.
Article in English | MEDLINE | ID: mdl-37518466

ABSTRACT

A morphological description of the last (fifth) instar larva of Macrostemum floridum (Navás 1929), its life cycle, and feeding habits are provided. The study was conducted along the Khlong Yan Stream in Kaengkrung National Park, southern Thailand. Larval identification was achieved by the metamorphotype method of associating immature stages with the adult. A graph of head capsule widths for all instars is provided. Gut content analysis showed that the main food items were diatoms, green algae, and blue-green algae. The larvae construct fixed retreats and feed as collecting filterers.


Subject(s)
Holometabola , Insecta , Animals , Larva/anatomy & histology , Insecta/anatomy & histology , Thailand , Parks, Recreational , Habits
SELECTION OF CITATIONS
SEARCH DETAIL